Homo sapiens (human): 81887
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Entry
81887 CDS
T01001
Symbol
LAS1L, Las1, Las1-like, MRXSWTS, WTS, dJ475B7.2
Name
(RefSeq) ribosomal biogenesis protein LAS1L isoform 1
KO
K16912
ribosomal biogenesis protein LAS1
Organism
hsa
Homo sapiens (human)
Disease
H02267
Wilson-Turner syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03009 Ribosome biogenesis [BR:
hsa03009
]
81887 (LAS1L)
Ribosome biogenesis [BR:
hsa03009
]
Eukaryotic type
Pre-60S particles
5-FMC complex
81887 (LAS1L)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Las1
NOA36
Motif
Other DBs
NCBI-GeneID:
81887
NCBI-ProteinID:
NP_112483
OMIM:
300964
HGNC:
25726
Ensembl:
ENSP00000363944.3
UniProt:
Q9Y4W2
Structure
PDB
PDBj
LinkDB
All DBs
Position
X:complement(65512582..65534787)
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AA seq
734 aa
AA seq
DB search
MSWESGAGPGLGSQGMDLVWSAWYGKCVKGKGSLPLSAHGIVVAWLSRAEWDQVTVYLFC
DDHKLQRYALNRITVWRSRSGNELPLAVASTADLIRCKLLDVTGGLGTDELRLLYGMALV
RFVNLISERKTKFAKVPLKCLAQEVNIPDWIVDLRHELTHKKMPHINDCRRGCYFVLDWL
QKTYWCRQLENSLRETWELEEFREGIEEEDQEEDKNIVVDDITEQKPEPQDDGKSTESDV
KADGDSKGSEEVDSHCKKALSHKELYERARELLVSYEEEQFTVLEKFRYLPKAIKAWNNP
SPRVECVLAELKGVTCENREAVLDAFLDDGFLVPTFEQLAALQIEYEDGQTEVQRGEGTD
PKSHKNVDLNDVLVPKPFSQFWQPLLRGLHSQNFTQALLERMLSELPALGISGIRPTYIL
RWTVELIVANTKTGRNARRFSAGQWEARRGWRLFNCSASLDWPRMVESCLGSPCWASPQL
LRIIFKAMGQGLPDEEQEKLLRICSIYTQSGENSLVQEGSEASPIGKSPYTLDSLYWSVK
PASSSFGSEAKAQQQEEQGSVNDVKEEEKEEKEVLPDQVEEEEENDDQEEEEEDEDDEDD
EEEDRMEVGPFSTGQESPTAENARLLAQKRGALQGSAWQVSSEDVRWDTFPLGRMPGQTE
DPAELMLENYDTMYLLDQPVLEQRLEPSTCKTDTLGLSCGVGSGNCSNSSSSNFEGLLWS
QGQLHGLKTGLQLF
NT seq
2205 nt
NT seq
+upstream
nt +downstream
nt
atgtcgtgggaatccggggccgggccaggtctaggttcccaggggatggatctcgtgtgg
agtgcgtggtacggaaagtgcgttaaagggaaagggtcgttgccactctcggcccacggc
atcgtggtcgcctggctcagcagggccgagtgggaccaggtgacggtttatctgttctgt
gacgaccataagttgcagcggtacgcgcttaaccgcatcacggtgtggaggagcaggtca
ggcaacgaactccctctggcagtggcttctactgctgacctgatacgctgtaagctcttg
gatgtaactggtggcttgggcactgatgaacttagactgctctatggcatggcattggtc
aggtttgtgaatcttatctcagagaggaagacaaagtttgccaaggtccccctcaagtgt
ctggctcaagaggtaaatattccggattggattgttgaccttcgccatgagttgacccac
aagaaaatgccccatataaatgactgccgcagaggctgctactttgtcctggattggctc
cagaagacctattggtgccgccaactggagaacagcctgagagagacctgggagttggag
gagttcagggaagggatagaggaagaggatcaagaggaagataagaacattgttgttgat
gacatcacagaacagaaaccagagcctcaggatgatgggaaaagtacggagtcagatgta
aaggccgatggagacagcaaaggcagcgaagaggtggattctcattgcaaaaaggccctg
agtcataaagagctatatgaaagagcccgagaactgctggtatcatacgaagaggagcag
tttacggtgctggagaaatttaggtatttacctaaggccattaaggcgtggaataacccg
tccccacgtgtagaatgtgtcctggcagagctcaagggcgttacatgcgagaacagggag
gctgtgctggatgcttttctggatgatggcttccttgtccccacatttgaacagttggca
gctttgcagatagaatatgaagatggtcagactgaggtccagagaggggaaggtactgac
ccaaagtcacacaaaaacgtggacttgaatgacgtcctggtgccaaagccgttctctcag
ttctggcagcccctgctcaggggcctgcactcccagaacttcacgcaggccctattggag
aggatgctctctgaactgccagccttggggatcagcgggatccggcctacctacatcctc
agatggaccgttgaactgatcgtggccaacaccaagactggacggaatgctcgccgattt
tctgcaggccagtgggaagcaagaaggggctggaggctgttcaactgctccgcctccctt
gactggccccggatggttgagtcctgcttgggctcaccttgctgggccagcccccaactc
cttcggatcatcttcaaagccatggggcagggcctgccagacgaggagcaggagaagctg
ctgcgcatctgttccatttatacccagagtggagaaaacagcctggtgcaggagggctct
gaggcctcccccattgggaagtctccatatacactagacagcctgtattggagcgtcaag
ccagccagctccagcttcgggtctgaagcaaaggcccagcaacaggaggagcagggcagt
gttaatgatgtcaaggaagaggagaaggaggagaaagaggtcttgccagaccaggtagag
gaggaggaagaaaatgatgaccaagaggaggaagaggaggatgaagatgatgaagatgat
gaagaggaagacagaatggaggtggggcctttctctacagggcaagagtcccccactgcc
gagaatgctaggcttctggcccagaaaagaggagctttgcagggctctgcatggcaggtt
agctcagaagacgtgcgatgggacacatttcccctaggccgaatgccaggtcagaccgag
gacccagcagagctcatgctggagaattatgacaccatgtatcttttggaccagcctgtg
ctagagcagcggctggaaccctcaacatgcaagactgacaccttgggcctgagctgtggt
gtcggcagtggcaactgcagcaacagcagcagcagcaacttcgagggccttctctggagc
caggggcagctgcatgggctcaaaactggcctgcagctcttctga
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